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This is a Phase 4, observational, open study in patients whom their doctor for clinical practice prescribes levamlodipine. No medication was provided by the sponsor. The planned observation time is 8 weeks. The 8 weeks of observation involves an evaluation of baseline followed by information gathered from the assessment visits at week 4 and week 8, or clinical practice.
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| Measure | Description | Time Frame |
|---|---|---|
| Effect of therapy in the management of hypertension and other cardiovascular diseases | The change from Baseline in Blood Pressure at 8 weeks will be measure to evaluate th efficacy of the therapy. | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants with Adverse Events as a Measure of Safety and Tolerability | The number of Participants with Serious and Non- seriuous Adverse Events wil be mesure to evaluate the tolerability and safety profile in 8 weeks follow up. | 8 weeks |
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Inclusion Criteria:
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Primary care adults in Colombia
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sandra M Casiano, M.D. | Contact | 57-3174049763 | scasiano@closterpharma.com | |
| Harold Mejia | Contact | 57-2264757 | hmejia@closterpharma.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Country Club Bogota | Recruiting | Bogotá | Colombia |
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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